N-Isopropyl-4-nitrobenzenesulfonamide

95%

Reagent Code: #219024
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CAS Number 23530-48-5

science Other reagents with same CAS 23530-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.27 g/mol
Formula C₉H₁₂N₂O₄S
badge Registry Numbers
MDL Number MFCD00458973
thermostat Physical Properties
Melting Point 112-113 °C
Boiling Point 388.1±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.318±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. Its electron-withdrawing nitro group and sulfonamide functionality make it suitable for nucleophilic substitution reactions, enabling the introduction of various amine or heterocyclic moieties. It is also employed in the development of protease inhibitors and other biologically active molecules due to the sulfonamide group's prevalence in medicinal chemistry. Additionally, it can act as a reagent or building block in the synthesis of dyes and functional materials where controlled reactivity and stability are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,710.00
inventory 250mg
10-20 days ฿3,300.00
inventory 1g
10-20 days ฿10,800.00

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N-Isopropyl-4-nitrobenzenesulfonamide
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. Its electron-withdrawing nitro group and sulfonamide functionality make it suitable for nucleophilic substitution reactions, enabling the introduction of various amine or heterocyclic moieties. It is also employed in the development of protease inhibitors and other biologically active molecules due to the sulfonamide group's prevalence in medicinal chemis

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfonamide-based pharmaceuticals and agrochemicals. Its electron-withdrawing nitro group and sulfonamide functionality make it suitable for nucleophilic substitution reactions, enabling the introduction of various amine or heterocyclic moieties. It is also employed in the development of protease inhibitors and other biologically active molecules due to the sulfonamide group's prevalence in medicinal chemistry. Additionally, it can act as a reagent or building block in the synthesis of dyes and functional materials where controlled reactivity and stability are required.

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